Class I · High risk Terminated
Mia's Bakery Black Sesame Mochi Wt
Reason Black Sesame Mochi does not declare milk powder
Mia's Bakery Bahn Xu Dua Wt recall
Recalled by Mai's Bakery, Corp · Monterey Park, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Banh Xu Dua Zuda Cake does not declare coconut on the product label, although is it visible.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Mia's Bakery Bahn Xu Dua Wt. 7 oz./198.5 gram UPC: 8 50660 00003 8 Ings: Glutinous Rice Flour, Sugar, Mung Bean, Soy Bean Oil, Water, Sesame Oil, Sodium Benzoate, Black Color, FD & C Yellow 5 & 6, Red #4 and Blue #1. Keep refrigerated after opening 1965 Potrero Grande Dr. #1 & H, Monterey Park, CA 91754 Tel: (626) 307-9629 Fax: (626) 307-9630
Quantity: 39 packages
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No codes
Where it was sold
Arizona California Michigan Nebraska
FDA's distribution note: Firm has 1 distributor located in Los Angeles, CA and further distributed product to 6 markets located in Arizona, California, Denver, Michigan, Nebraska, and Arizona
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Mai's Bakery, Corp
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 18, 2022
- In FDA report of
- Jun 29, 2022
- Terminated
- Jun 29, 2022
- FDA recall number
- F-1342-2022 · event 90235
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.